Canonical Allele Identifier:
CA1697889669
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897408A= , CM000669.2:g.30897408A= | GRCh38 |
| NC_000007.13:g.30937023A= , CM000669.1:g.30937023A= | GRCh37 |
| NC_000007.12:g.30903548A= | NCBI36 |
| NG_007475.2:g.49015A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000509504.2:c.621+14415A= |